rs7177289

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rs7177289 has 2 RGD Records - Homo sapiens

  
Variant Page
Assembly
Chr
Position
Type
Reference Nucleotide
Variant Nucleotide
Location Name
Is Damaging?
Visualize
1. View more GRCh38 15 58,387,985 - 58,387,986 snv C T - -
2. View more GRCh38 15 58,387,985 - 58,387,986 snv C C - -